A p-n WO3/SnSe2 Heterojunction for Efficient Photo-assisted Electrocatalysis of the Oxygen Evolution Reaction

被引:26
作者
Bai, Ling [1 ,2 ]
Jia, Shijie [1 ]
Gao, Yidan [1 ]
Li, Chuan [1 ]
Chen, Xin [1 ]
Zhou, Shuang [1 ]
Han, Junwen [2 ]
Yang, Fengchun [1 ]
Zhang, Xin [1 ]
Lu, Siyu [3 ]
机构
[1] Northwest Univ, Coll Chem & Mat Sci, Xian 710127, Peoples R China
[2] Jinchuan Grp Co Ltd, Jinchang 737100, Peoples R China
[3] Zhengzhou Univ, Coll Chem, Green Catalysis Ctr, Zhengzhou 450001, Peoples R China
基金
中国国家自然科学基金;
关键词
active species; oxygen evolution reaction; photo-assisted electrocatalysis; photogenerated charge separation; p-n WO3; SnSe2; heterojunction; DOUBLE HYDROXIDE NANOSHEETS; HIGHLY-EFFICIENT; CARBON NANOTUBES; WATER OXIDATION; WO3; PHOTOANODE; THIN-FILMS; PERFORMANCE; NANOPARTICLES; EXFOLIATION; VACANCIES;
D O I
10.1002/eem2.12456
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Water splitting is important to the conversion and storage of renewable energy, but slow kinetics of the oxygen evolution reaction (OER) greatly limits its utility. Here, under visible light illumination, the p-n WO3/SnSe2 (WS) heterojunction significantly activates OER catalysis of CoFe-layered double hydroxide (CF)/carbon nanotubes (CNTs). Specifically, the catalyst achieves an overpotential of 224 mV at 10 mA cm(-2) and a small Tafel slope of 47 mV dec(-1), superior to RuO2 and most previously reported transition metal-based OER catalysts. The p-n WS heterojunction shows strong light absorption to produce photogenerated carriers. The photogenerated holes are trapped by CF to suppresses the charge recombination and facilitate charge transfer, which accelerates OER kinetics and boost the activity for the OER. This work highlights the possibility of using heterojunctions to activate OER catalysis and advances the design of energy-efficient catalysts for water oxidation systems using solar energy.
引用
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页数:8
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